| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:69829479-69829737 | Common:1; Rare:104 | ||||
| chr2:69914618-69914716 | Rare:28 | ||||
| chr2:70087414-70087762 | Rare:138 | ||||
| chr2:70087933-70088089 | Rare:38 | ||||
| chr2:70190986-70191127 | Rare:34 | ||||
| chr2:70258030-70258231 | Common:2; Rare:71 | ||||
| chr2:70293645-70293821 | Common:2; Rare:64 | ||||
| chr2:71068526-71068654 | Rare:64 | ||||
| chr2:71130221-71130666 | Common:6; Rare:125; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:73071707-73071843 | Common:2; Rare:50 | ||||
| chr2:73214140-73214333 | Common:1; Rare:75 | ||||
| chr2:73214483-73214532 | Rare:22 | ||||
| chr2:73233200-73233456 | Common:1; Rare:66 | ||||
| chr2:73234250-73234364 | Common:1; Rare:40 | ||||
| chr2:73385710-73386099 | Common:4; Rare:196; Clinvar:18; Clinvar (benign):9; Clinvar (pathogenic):1 |